SPARC announces submission of IND Application for SBO-154 to USFDA
The IND application supports the next phase of development of SBO-154
The IND application supports the next phase of development of SBO-154
Alkem Medtech to acquire 100% stake of Bombay Ortho
The product is being recalled because the infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL single-dose bag, while the aluminum overwrap packaging correctly identifies the product as Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 m
The basket acquired, comprises of 13 ANDAs, which are approved by the USFDA and 1 ANDA, which is pending approval from the USFDA
This is Senores' second API manufacturing facility adding significantly to the existing API manufacturing capabilities.
Cipla Limited has received final approval from the USFDA for the New Drug Application submitted for ‘Nilotinib Capsules 50, 150 and 200 mg’
the inspection conducted from January 27 to January 31, 2025
Offers affordable, high-quality solutions for diabetes care
Revenue up 11% to Rs 5,768 crore as compared to Rs 5,197 crore
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